Canonical Allele Identifier: CA2613426607

Gene: NDUFS3

Linked Data

• gnomAD v4: 11-47582289-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.47582289G>A , CM000673.2:g.47582289G>A	GRCh38
NC_000011.9:g.47603841G>A , CM000673.1:g.47603841G>A	GRCh37
NC_000011.8:g.47560417G>A	NCBI36
NG_011946.1:g.8280G>A
NG_011946.2:g.8280G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263774.9:c.508-60G>A MANE Select	ENSP00000263774.4:n.508-60G>A
ENST00000531351.2:n.1643G>A
ENST00000677462.1:n.2982-60G>A
ENST00000678975.1:n.2765-60G>A
ENST00000263774.8:c.508-60G>A	ENSP00000263774.4:n.508-60G>A
ENST00000524568.1:n.611-60G>A
ENST00000525212.1:n.163-60G>A
ENST00000525378.5:n.446-60G>A
ENST00000527178.1:n.48G>A
ENST00000533507.5:n.1402-60G>A
NM_004551.2:c.508-60G>A	NP_004542.1:n.508-60G>A
NM_004551.3:c.508-60G>A MANE Select	NP_004542.1:n.508-60G>A